view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ME1_chr6_83205402_83436051 | 83298931 | GTTTTTTT others(6): Show |
G | intron_variant | MODIFIER | HG02723.hp1 HG03579.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | 272 | 0.0074 | -13 | c.704 others(32): Show |
ME1 | ENSG00000065833.9 | transcript | ENST00000369705.4 | protein_coding | 6/13 | chr6 | TogoVar | |||||||
ME2_chr18_50874118_50959257 | 50951866 | CAAAAAAA others(6): Show |
C | 3_prime_UTR_variant | MODIFIER | HG02056.hp1 NA18957.hp2 NA19000.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0027a0001c0001t0071a0001c0001t0075 | a0001c0001t0027g0042 a0001c0001t0027g0047 a0001c0001t0071g0045 others(1): Show |
4 | 342 | 0.0117 | -13 | c.*47 others(24): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 16/16 | 4707 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ME2_chr18_50874118_50959257 | 50959166 | CTCCCTCC others(6): Show |
C | downstream_gene_variant | MODIFIER | NA18995.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0092 | 1 | 342 | 0.0029 | -13 | c.*11 others(26): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4910 | chr18 | TogoVar | |||||||
MEAF6_chr1_37484993_37519766 | 37495691 | AAAAAACA others(6): Show |
A | intron_variant | MODIFIER | HG02258.hp2 HG02717.hp1 |
a0001 | a0001c0001 | a0001c0001t0014 | a0001c0001t0014g0353 a0001c0001t0014g0355 |
2 | 428 | 0.0047 | -13 | c.567 others(28): Show |
MEAF6 | ENSG00000163875.16 | transcript | ENST00000296214.10 | protein_coding | 6/6 | chr1 | TogoVar | |||||||
MEAF6_chr1_37484993_37519766 | 37502316 | TCCTCCTG others(6): Show |
T | intron_variant | MODIFIER | HG01069.hp1 NA18522.hp2 |
a0001 | a0001c0001 | a0001c0001t0024 | a0001c0001t0024g0283 a0001c0001t0024g0284 |
2 | 428 | 0.0047 | -13 | c.341 others(28): Show |
MEAF6 | ENSG00000163875.16 | transcript | ENST00000296214.10 | protein_coding | 4/6 | chr1 | TogoVar | |||||||
MEAF6_chr1_37484993_37519766 | 37517782 | ACAAGCAT others(6): Show |
A | upstream_gene_variant | MODIFIER | HG01516.hp2 | a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0037 | 1 | 428 | 0.0023 | -13 | c.-30 others(24): Show |
MEAF6 | ENSG00000163875.16 | transcript | ENST00000296214.10 | protein_coding | 3017 | chr1 | TogoVar | |||||||
MECOM_chr3_169078507_169668712 | 169191719 | AAAAAGAA others(6): Show |
A | intron_variant | MODIFIER | HG01099.hp1 HG03098.hp2 HG03831.hp2 others(4): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0010a0001c0001t0021a0001c0001t0028others(4): Show | a0001c0001t0010g0079 a0001c0001t0021g0152 a0001c0001t0028g0007 others(4): Show |
7 | 160 | 0.0438 | -13 | c.376 others(32): Show |
MECOM | ENSG00000085276.19 | transcript | ENST00000651503.2 | protein_coding | 2/16 | chr3 | TogoVar | |||||||
MECOM_chr3_169078507_169668712 | 169382861 | AAAATAAA others(6): Show |
A | intron_variant | MODIFIER | HG02109.hp2 HG02257.hp2 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0007a0001c0001t0013a0001c0001t0014 | a0001c0001t0007g0135 a0001c0001t0013g0050 a0001c0001t0014g0148 |
3 | 160 | 0.0188 | -13 | c.38- others(28): Show |
MECOM | ENSG00000085276.19 | transcript | ENST00000651503.2 | protein_coding | 1/16 | chr3 | TogoVar | |||||||
MECOM_chr3_169078507_169668712 | 169418780 | AGCCAATA others(6): Show |
A | intron_variant | MODIFIER | HG00438.hp2 HG00544.hp2 HG00741.hp2 others(22): Show |
a0001a0003 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(15): Show | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0001g0053 others(22): Show |
25 | 160 | 0.1563 | -13 | c.38- others(30): Show |
MECOM | ENSG00000085276.19 | transcript | ENST00000651503.2 | protein_coding | 1/16 | chr3 | TogoVar | |||||||
MECOM_chr3_169078507_169668712 | 169472512 | GGAAAGGA others(6): Show |
G | intron_variant | MODIFIER | HG04228.hp1 | a0001 | a0001c0003 | a0001c0003t0002 | a0001c0003t0002g0078 | 1 | 160 | 0.0063 | -13 | c.38- others(30): Show |
MECOM | ENSG00000085276.19 | transcript | ENST00000651503.2 | protein_coding | 1/16 | chr3 | TogoVar | |||||||
MECOM_chr3_169078507_169668712 | 169499346 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG01099.hp1 HG02615.hp1 NA18522.hp1 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0003a0001c0001t0005a0001c0001t0016others(2): Show | a0001c0001t0003g0031 a0001c0001t0005g0104 a0001c0001t0016g0064 others(2): Show |
5 | 160 | 0.0313 | -13 | c.38- others(32): Show |
MECOM | ENSG00000085276.19 | transcript | ENST00000651503.2 | protein_coding | 1/16 | chr3 | TogoVar | |||||||
MECOM_chr3_169078507_169668712 | 169659440 | ATTTTTTT others(6): Show |
A | intron_variant | MODIFIER | HG01255.hp2 HG02258.hp1 HG02723.hp1 others(9): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(2): Show | a0001c0001t0006a0001c0001t0008a0001c0001t0009others(8): Show | a0001c0001t0006g0123 a0001c0001t0008g0110 a0001c0001t0009g0141 others(9): Show |
12 | 160 | 0.0750 | -13 | c.37+ others(28): Show |
MECOM | ENSG00000085276.19 | transcript | ENST00000651503.2 | protein_coding | 1/16 | chr3 | TogoVar | |||||||
MECOM_chr3_169078507_169668712 | 169663517 | TCTCTCTC others(6): Show |
T | 5_prime_UTR_variant | MODIFIER | NA18952.hp1 NA18988.hp1 |
a0002a0003 | a0002c0002a0003c0005 | a0002c0002t0018a0003c0005t0018 | a0002c0002t0018g0008 a0003c0005t0018g0009 |
2 | 160 | 0.0125 | -13 | c.-15 others(22): Show |
MECOM | ENSG00000085276.19 | transcript | ENST00000651503.2 | protein_coding | 1/17 | 146 | chr3 | TogoVar | ||||||
MECOM_chr3_169078507_169668712 | 169663521 | TCTCTCTC others(6): Show |
T | 5_prime_UTR_variant | MODIFIER | HG01175.hp1 | a0001 | a0001c0001 | a0001c0001t0023 | a0001c0001t0023g0002 | 1 | 160 | 0.0063 | -13 | c.-16 others(22): Show |
MECOM | ENSG00000085276.19 | transcript | ENST00000651503.2 | protein_coding | 1/17 | 150 | chr3 | TogoVar | ||||||
MECP2_chrX_154016573_154102717 | 154052454 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG02040.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0153 | 1 | 230 | 0.0044 | -13 | c.27- others(30): Show |
MECP2 | ENSG00000169057.25 | transcript | ENST00000303391.11 | protein_coding | 2/3 | chrX | TogoVar | |||||||
MED12L_chr3_151080664_151441653 | 151085743 | GGCGAGCC others(6): Show |
G | 5_prime_UTR_variant | MODIFIER | HG01081.hp1 | a0004 | a0004c0016 | a0004c0016t0057 | a0004c0016t0057g0099 | 1 | 280 | 0.0036 | -13 | c.-32 others(22): Show |
MED12L | ENSG00000144893.13 | transcript | ENST00000687756.1 | protein_coding | 1/45 | 1169 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
MED12L_chr3_151080664_151441653 | 151115327 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG02145.hp1 HG02486.hp2 HG02698.hp2 others(6): Show |
a0001 | a0001c0001a0001c0007a0001c0008others(5): Show | a0001c0001t0007a0001c0007t0001a0001c0007t0009others(6): Show | a0001c0001t0007g0159 a0001c0007t0001g0040 a0001c0007t0009g0035 others(6): Show |
9 | 280 | 0.0321 | -13 | c.100 others(28): Show |
MED12L | ENSG00000144893.13 | transcript | ENST00000687756.1 | protein_coding | 2/44 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
MED12L_chr3_151080664_151441653 | 151218866 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG01192.hp2 HG03130.hp2 HG04228.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0001t0007a0001c0001t0008others(2): Show | a0001c0001t0003g0140 a0001c0001t0003g0141 a0001c0001t0007g0159 others(3): Show |
6 | 280 | 0.0214 | -13 | c.225 others(34): Show |
MED12L | ENSG00000144893.13 | transcript | ENST00000687756.1 | protein_coding | 16/44 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
MED12L_chr3_151080664_151441653 | 151269428 | CACACACA others(6): Show |
C | intron_variant | MODIFIER | HG04115.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0276 | 1 | 280 | 0.0036 | -13 | c.225 others(34): Show |
MED12L | ENSG00000144893.13 | transcript | ENST00000687756.1 | protein_coding | 16/44 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
MED12L_chr3_151080664_151441653 | 151307573 | GTGTGTGT others(6): Show |
G | intron_variant | MODIFIER | HG04115.hp1 | a0002 | a0002c0003 | a0002c0003t0004 | a0002c0003t0004g0165 | 1 | 280 | 0.0036 | -13 | c.225 others(34): Show |
MED12L | ENSG00000144893.13 | transcript | ENST00000687756.1 | protein_coding | 16/44 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
MED12L_chr3_151080664_151441653 | 151354140 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG00423.hp1 | a0002 | a0002c0003 | a0002c0003t0004 | a0002c0003t0004g0091 | 1 | 280 | 0.0036 | -13 | c.239 others(30): Show |
MED12L | ENSG00000144893.13 | transcript | ENST00000687756.1 | protein_coding | 17/44 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
MED13L_chr12_115953576_116282693 | 116031727 | AAAGAAAA others(6): Show |
A | intron_variant | MODIFIER | HG03017.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0076 | 1 | 254 | 0.0039 | -13 | c.480 others(30): Show |
MED13L | ENSG00000123066.9 | transcript | ENST00000281928.9 | protein_coding | 4/30 | chr12 | TogoVar | |||||||
MED13L_chr12_115953576_116282693 | 116031737 | AAAGAAAA others(6): Show |
A | intron_variant | MODIFIER | HG01346.hp2 HG03017.hp2 NA18963.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0161 a0001c0001t0001g0216 a0001c0002t0002g0039 others(1): Show |
4 | 254 | 0.0158 | -13 | c.480 others(30): Show |
MED13L | ENSG00000123066.9 | transcript | ENST00000281928.9 | protein_coding | 4/30 | chr12 | TogoVar | |||||||
MED13L_chr12_115953576_116282693 | 116103999 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | NA20752.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0186 | 1 | 254 | 0.0039 | -13 | c.396 others(30): Show |
MED13L | ENSG00000123066.9 | transcript | ENST00000281928.9 | protein_coding | 3/30 | chr12 | TogoVar | |||||||
MED13L_chr12_115953576_116282693 | 116106420 | AAGAAATG others(6): Show |
A | intron_variant | MODIFIER | HG02717.hp2 HG02922.hp2 HG03195.hp2 others(2): Show |
a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0095 a0001c0005t0001g0096 a0001c0005t0001g0097 others(2): Show |
5 | 254 | 0.0197 | -13 | c.395 others(30): Show |
MED13L | ENSG00000123066.9 | transcript | ENST00000281928.9 | protein_coding | 3/30 | chr12 | TogoVar | |||||||
MED13_chr17_61937605_62070278 | 61937898 | CAAAAAAA others(6): Show |
C | downstream_gene_variant | MODIFIER | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(89): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0009others(10): Show | a0001c0001t0001g0187 a0001c0001t0001g0282 a0001c0002t0001g0001 others(89): Show |
92 | 326 | 0.2822 | -13 | c.*85 others(24): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 4706 | chr17 | TogoVar | |||||||
MED13_chr17_61937605_62070278 | 61944288 | GTAAAGTC others(6): Show |
G | 3_prime_UTR_variant | MODIFIER | HG03017.hp2 | a0001 | a0001c0001 | a0001c0001t0021 | a0001c0001t0021g0129 | 1 | 326 | 0.0031 | -13 | c.*21 others(24): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 30/30 | 2167 | chr17 | TogoVar | ||||||
MED13_chr17_61937605_62070278 | 61998839 | TCCTCCCA others(6): Show |
T | intron_variant | MODIFIER | HG02572.hp1 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0080 | 1 | 326 | 0.0031 | -13 | c.196 others(32): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 9/29 | chr17 | TogoVar | |||||||
MED13_chr17_61937605_62070278 | 62015952 | ATATTTTT others(6): Show |
A | intron_variant | MODIFIER | HG01891.hp2 HG02602.hp2 NA18522.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003a0001c0004 | a0001c0001t0002a0001c0001t0010a0001c0003t0001others(1): Show | a0001c0001t0002g0130 a0001c0001t0010g0150 a0001c0003t0001g0112 others(2): Show |
5 | 326 | 0.0153 | -13 | c.128 others(32): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | TogoVar | |||||||
MED13_chr17_61937605_62070278 | 62015954 | ATTTTTTT others(6): Show |
A | intron_variant | MODIFIER | HG02965.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0089 | 1 | 326 | 0.0031 | -13 | c.128 others(32): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | TogoVar | |||||||
MED13_chr17_61937605_62070278 | 62037955 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(80): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0003a0001c0006others(5): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0010others(13): Show | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0119 others(80): Show |
83 | 326 | 0.2546 | -13 | c.471 others(30): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | TogoVar | |||||||
MED13_chr17_61937605_62070278 | 62048398 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG02145.hp1 HG02257.hp1 HG03540.hp2 others(3): Show |
a0001a0004a0005 | a0001c0007a0001c0021a0004c0011others(1): Show | a0001c0007t0005a0001c0021t0017a0004c0011t0001others(1): Show | a0001c0007t0005g0009 a0001c0007t0005g0010 a0001c0007t0005g0012 others(3): Show |
6 | 326 | 0.0184 | -13 | c.470 others(30): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | TogoVar | |||||||
MED15_chr22_20502610_20592619 | 20505579 | AAAAAAAA others(6): Show |
A | upstream_gene_variant | MODIFIER | HG02300.hp2 NA18957.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0013 a0001c0001t0001g0056 |
2 | 341 | 0.0059 | -13 | c.-20 others(24): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2030 | chr22 | TogoVar | |||||||
MED15_chr22_20502610_20592619 | 20570746 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG02165.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0312 | 1 | 341 | 0.0029 | -13 | c.115 others(32): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
MED1_chr17_39399285_39456263 | 39414634 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG00738.hp2 HG01943.hp2 HG01975.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004 | a0001c0001t0002g0004 a0001c0001t0002g0195 a0001c0001t0002g0214 others(3): Show |
7 | 280 | 0.0250 | -13 | c.149 others(30): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 16/16 | chr17 | TogoVar | |||||||
MED28_chr4_17609641_17639105 | 17632043 | ATTTTTTT others(6): Show |
A | 3_prime_UTR_variant | MODIFIER | NA18946.hp2 | a0001 | a0001c0001 | a0001c0001t0077 | a0001c0001t0077g0002 | 1 | 328 | 0.0031 | -13 | c.*82 others(24): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4/4 | 8277 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
MED28_chr4_17609641_17639105 | 17638134 | CTTTTTTT others(6): Show |
C | downstream_gene_variant | MODIFIER | HG02055.hp1 HG02258.hp2 HG02486.hp1 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0010a0001c0001t0034a0001c0001t0035others(4): Show | a0001c0001t0010g0009 a0001c0001t0010g0075 a0001c0001t0010g0076 others(7): Show |
13 | 328 | 0.0396 | -13 | c.*14 others(26): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 4030 | chr4 | TogoVar | |||||||
MED29_chr19_39386378_39405641 | 39393072 | CTTTCTTT others(6): Show |
C | intron_variant | MODIFIER | HG01069.hp2 HG03579.hp1 NA18969.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(2): Show | a0001c0001t0001g0112 a0001c0001t0003g0110 a0001c0001t0003g0148 others(3): Show |
6 | 388 | 0.0155 | -13 | c.276 others(28): Show |
MED29 | ENSG00000063322.15 | transcript | ENST00000315588.11 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
MED4_chr13_48070724_48100104 | 48085170 | ATTTTTTT others(6): Show |
A | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(139): Show |
a0001a0003 | a0001c0001a0001c0005a0003c0004 | a0001c0001t0001a0001c0001t0005a0001c0001t0010others(6): Show | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(53): Show |
142 | 408 | 0.3480 | -13 | c.363 others(30): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | TogoVar | |||||||
MED6_chr14_70578221_70605655 | 70592478 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG02723.hp1 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0159 | 1 | 406 | 0.0025 | -13 | c.466 others(28): Show |
MED6 | ENSG00000133997.12 | transcript | ENST00000256379.10 | protein_coding | 5/7 | chr14 | TogoVar | |||||||
MED8_chr1_43378917_43394800 | 43392083 | CAAAAAAA others(6): Show |
C | upstream_gene_variant | MODIFIER | HG00423.hp2 HG02027.hp1 HG02083.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 5 | 382 | 0.0131 | -13 | c.-23 others(24): Show |
MED8 | ENSG00000159479.17 | transcript | ENST00000372457.9 | protein_coding | 2284 | chr1 | TogoVar | |||||||
MEF2A_chr15_99560984_99721488 | 99610414 | CCCCCCCC others(6): Show |
C | intron_variant | MODIFIER | HG02895.hp2 HG02897.hp1 NA18986.hp1 |
a0001a0006 | a0001c0001a0006c0015 | a0001c0001t0045a0006c0015t0004 | a0001c0001t0045g0226 a0006c0015t0004g0154 a0006c0015t0004g0155 |
3 | 376 | 0.0080 | -13 | c.-14 others(34): Show |
MEF2A | ENSG00000068305.19 | transcript | ENST00000557942.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
MEF2C_chr5_88712117_88888184 | 88786673 | GCTACATA others(6): Show |
G | intron_variant | MODIFIER | HG01891.hp2 HG03225.hp2 |
a0001 | a0001c0001 | a0001c0001t0019a0001c0001t0024 | a0001c0001t0019g0067 a0001c0001t0024g0066 |
2 | 302 | 0.0066 | -13 | c.258 others(32): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 3/10 | chr5 | TogoVar | |||||||
MEF2C_chr5_88712117_88888184 | 88873708 | ATTTTTTT others(6): Show |
A | intron_variant | MODIFIER | NA18989.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0024 | 1 | 302 | 0.0033 | -13 | c.-14 others(32): Show |
MEF2C | ENSG00000081189.17 | transcript | ENST00000504921.7 | protein_coding | 1/10 | chr5 | TogoVar | |||||||
MEGF10_chr5_127285796_127466222 | 127320464 | TAGATACC others(6): Show |
T | intron_variant | MODIFIER | HG00323.hp1 HG00558.hp2 HG02040.hp2 others(20): Show |
a0001a0007 | a0001c0005a0001c0006a0001c0015others(1): Show | a0001c0005t0007a0001c0005t0016a0001c0006t0001others(4): Show | a0001c0005t0007g0020 a0001c0005t0007g0022 a0001c0005t0007g0023 others(20): Show |
23 | 268 | 0.0858 | -13 | c.-18 others(32): Show |
MEGF10 | ENSG00000145794.17 | transcript | ENST00000503335.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
MEGF11_chr15_65890299_66258750 | 65935322 | GAAAAAAA others(6): Show |
G | intron_variant | MODIFIER | HG03579.hp1 | a0002 | a0002c0005 | a0002c0005t0002 | a0002c0005t0002g0152 | 1 | 176 | 0.0057 | -13 | c.128 others(32): Show |
MEGF11 | ENSG00000157890.19 | transcript | ENST00000395614.6 | protein_coding | 10/25 | chr15 | TogoVar | |||||||
MEGF11_chr15_65890299_66258750 | 65965588 | CTTTCTTT others(6): Show |
C | intron_variant | MODIFIER | HG00099.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0166 | 1 | 176 | 0.0057 | -13 | c.900 others(28): Show |
MEGF11 | ENSG00000157890.19 | transcript | ENST00000395614.6 | protein_coding | 8/25 | chr15 | TogoVar | |||||||
MEGF11_chr15_65890299_66258750 | 66082425 | TAAAAAAA others(6): Show |
T | intron_variant | MODIFIER | HG00741.hp2 | a0004 | a0004c0004 | a0004c0004t0003 | a0004c0004t0003g0074 | 1 | 176 | 0.0057 | -13 | c.394 others(32): Show |
MEGF11 | ENSG00000157890.19 | transcript | ENST00000395614.6 | protein_coding | 5/25 | chr15 | TogoVar | |||||||
MEGF11_chr15_65890299_66258750 | 66082457 | AAAAAAAA others(6): Show |
A | intron_variant | MODIFIER | HG01516.hp2 HG02083.hp1 HG02572.hp1 others(2): Show |
a0001a0006a0011 | a0001c0001a0001c0021a0006c0006others(1): Show | a0001c0001t0001a0001c0001t0008a0001c0021t0008others(2): Show | a0001c0001t0001g0145 a0001c0001t0008g0175 a0001c0021t0008g0165 others(2): Show |
5 | 176 | 0.0284 | -13 | c.394 others(32): Show |
MEGF11 | ENSG00000157890.19 | transcript | ENST00000395614.6 | protein_coding | 5/25 | chr15 | TogoVar | |||||||
MEGF11_chr15_65890299_66258750 | 66082461 | AAAAAAAT others(6): Show |
A | intron_variant | MODIFIER | HG04199.hp2 NA19043.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0005 | a0001c0001t0002g0171 a0001c0001t0005g0023 |
2 | 176 | 0.0114 | -13 | c.394 others(32): Show |
MEGF11 | ENSG00000157890.19 | transcript | ENST00000395614.6 | protein_coding | 5/25 | chr15 | TogoVar |